Robust fluorescence sensing platform for detection of CD44 cells based on graphene oxide/gold nanoparticles
- Authors
- Jeong, Ha Young; Baek, Seung Hun; Chang, Sung-Jin; Cheon, Seon Ah; Park, Tae Jung
- Issue Date
- Nov-2015
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- Graphene oxide/gold nanoparticles (GO/AuNPs); Fluorescence sensing; Signal-to-background ratio enhancer; Aptamer; Hyaluronic acid binding domain of CD44
- Citation
- COLLOIDS AND SURFACES B-BIOINTERFACES, v.135, pp 309 - 315
- Pages
- 7
- Journal Title
- COLLOIDS AND SURFACES B-BIOINTERFACES
- Volume
- 135
- Start Page
- 309
- End Page
- 315
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/8925
- DOI
- 10.1016/j.colsurfb.2015.07.083
- ISSN
- 0927-7765
1873-4367
- Abstract
- Gold-coated graphene oxide hybrid material (GO/AuNPs) has exceptional physical and chemical properties like pi-pi stacking interaction and plays a role in quencher of fluorescence dye. Therefore, GO/AuNPs could enhance the signal-to-background ratio with fluorescence dye that was the point in this fluorescent biosensor. In this study, tetramethy1-6-carboxy-rhodamine (TAMRA)-labeled aptamers that specifically interact with the hyaluronic acid binding domain of CD44 were used as targets to investigate the applicability of the method. GO/AuNPs TAMRA-aptamer complexes could detect CD44 target cancer cells within a concentration range of 1 x 10(1) to 1 x 10(7) CFU/mL. A linear relationship was observed between target cell concentration and relative fluorescence intensity. The more mounted up CD44 target cell concentrations, relative fluorescence intensity of GO/AuNPs TAMRA-aptamer complexes was increased even more, which was superior to that of GO alone. Sensitivity of the detection system displayed a low detection limit of 1 x 10(1) CFU/mL. Additionally, this method is specific in that fluorescence is not much enhanced in CD44 negative cancer cell line. Thus, the fluorescence sensing based on GO/AuNPs could be developed to receptive and robust detection tool for various target molecules. (C) 2015 Elsevier B.V. All rights reserved.
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